Immunology In The CNS Flashcards

1
Q

Outline innate immunity

A

Non-specific, constitutive (continually expressed) and quick

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2
Q

What is involved in innate immunity

A

-anatomical (barriers)
-inflammation
-phagocytes and antigen-presenting cells
-PRRs recognising PAMPs

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3
Q

What cells are involved in innate immunity

A

-monocytes and macrophages
-dendritic cells
-neutrophils and other granulocytes (eosinophils, basophils, mast cells)

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4
Q

Outline adaptive immunity (humoral and cell-mediated)

A

Specific (diversity/polymorphism)
Induced- slower
Memory.

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5
Q

What lymphocytes are involved in adaptive immunity

A

T cells:
-helper
-cytotoxic
-regulatory
-memory
B cells:
-plasma (-> antibodies)
-memory

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6
Q

Outline recognition in the immune system

A

PAMPs (found on the microbial cell)
PRRs (innate cell)
BCRs and TCRs (T cells)

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7
Q

Outline myeloid cells of the immune system

A

Macrophage
Neutrophil
Dendritic cells
Eosinophils
Basophils

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8
Q

Outline macrophages

A

-phagocytosis
-bactericidal mechanisms
-antigen presentation
-cytokines production

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9
Q

Outline dendritic cells

A

-antigen uptake in periphery
-antigen presentation in lymph nodes
-cytokines production

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10
Q

Outline neutrophils
(Polymorphonuclear cells, PMNs)

A

-phagocytosis
-bactericidal mechanisms

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11
Q

Outline eosinophils

A

Killing of antibody-coated parasites

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12
Q

Outline basophils

A

-allergic responses
-augmentation of anti-parasite immunity

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13
Q

Outline lymphocytes

A

T and B lymphocytes cannot be distinguished by blood smear, instead by surface markers
Mostly small and inactive until they encounter the specific antigen that interacts with the receptor on their surface
T cells of subsets include CD4+ helper T cells and CD8+ cytotoxic T cells

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14
Q

What equipment can be used to analyse lymphocytes

A

Flow cytometry

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15
Q

What is cytokines role in the immune system?

A

Signalling, communication, activation and inhibition

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16
Q

What is in the meninges

A

Dura mater, arachnoid mater and pia mater

17
Q

Outline dura mater

A

Fenestrated blood vessels without tight junctions (likely exit for microbes in circulation)

18
Q

What cells are in the dura mater

A

Resident meningeal macrophages, DCs and other APCs sample and present antigen to surveying T cells

19
Q

Outline the arachnoid mater

A

Expresses tight junction proteins as a physical barrier between dura mater and CSF-filled subarachnoid space

20
Q

What is encephalitis

A

Crossing the BBB

21
Q

What is meningitis

A

Crossing thee blood- CSF barrier

22
Q

How can pathogens cross the BBB

A

-infecting the cells that compromise the barrier
-being passively transported across in intracellular vacuoles
-carriage across by infected white blood cells

23
Q

What happens when you have a CNS invasion of viruses

A

Increase in lymphocytes (mostly T cells) and monocytes in CSF, increase in protein, CSF remains mostly clear (‘aseptic meningitis’)

24
Q

What happens when you have a CNS invasion of bacteria

A

Rapid increase in neutrophils and protein, CSF becomes turbid (‘septic/purulent menigitis’)

25
Why is there limited success of a CNS pathogen invasion
Establishment of latency gives a mechanism for reactivation and later shedding Rabies- CNS invasion can be part of the route to shedding and invasion of lambic system can lead to helpful behaviour
26
What is inflammation for
Tissue homeostasis Tissue defence
27
Outline tissue homeostasis in inflammation
28
Outline tissue defence in inflammation
-production of cytotoxic substances -production of chemokines for recruitment of populations of immune cells -production of cytokines for coordination of immune response in local stromatol cells, vascular use and wider immune system
29
What are immunologically privileged sites
30
Give examples of immunologically privileged sites
31
Outline characteristics of immunologically privileged sites
-extracellular fluid does not pass through usual lymphatics- naive lymphocytes are excluded by the BBB -cytokines are produced such as anti-inflammatory TGF-b-skew towards Treg responses -expression of Fas ligand (FasL) induces apoptosis of Fas-bearing lymphocytes entering privileged sites
32
What is tolerance- deletion of self-reactive lymphocytes
-enormous diversity of specific receptors generated -most thymocytes express receptors that cannot interact with self MHC- these cells die in the thymus -positive selection preserves cells that can engage the MHC: peptide complex
33
How can damage to an immunologically privileged site induce an autoimmune response
34
Outline microglia
-resident macrophages (5-20% of all brain cells) -immune-privileged sites -a non-coding RNA, expressed in the CNS by developing neuronal cells, skews microglia towards an M2 state (less-inflammatory)
35
What is the function of M1 macrophages
36
What is the function of M2 macrophages
37
What is the role of microglia in neuroinflammation
Neuroprotection: -tropic factors -phagocytosis -debris clearance Neurotoxicity: -tissue inflammation -inflammatory cytokines -cell death/tissue damage